-
1
-
-
37049134337
-
-
For examples, see: E. M. Richards, J. C. Tebby, R. S. Ward and D. H. Williams, J. Chem. Soc. C, 1969, 1542-1544;
-
(1969)
J. Chem. Soc. C
, pp. 1542-1544
-
-
Richards, E.M.1
Tebby, J.C.2
Ward, R.S.3
Williams, D.H.4
-
2
-
-
0003317729
-
-
Y. Kataoka, K. Takai, K. Oshima and K. Utimoto, J. Org. Chem., 1992, 57, 1615-1618;
-
(1992)
J. Org. Chem.
, vol.57
, pp. 1615-1618
-
-
Kataoka, Y.1
Takai, K.2
Oshima, K.3
Utimoto, K.4
-
3
-
-
0000129330
-
-
M. A. G. M. Tinga, G. Schat, O. S. Akkerman, F. Bickelhaupt, E. Horn, H. Kooijman, W. J. J. Smeets and A. L. Spek, J. Am. Chem. Soc., 1993, 115, 2808-2817;
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 2808-2817
-
-
Tinga, M.A.G.M.1
Schat, G.2
Akkerman, O.S.3
Bickelhaupt, F.4
Horn, E.5
Kooijman, H.6
Smeets, W.J.J.7
Spek, A.L.8
-
4
-
-
0028934739
-
-
K. Harada, H. Urabe and F. Sato, Tetrahedron Lett., 1995, 36, 3203-3206;
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 3203-3206
-
-
Harada, K.1
Urabe, H.2
Sato, F.3
-
5
-
-
0242321221
-
-
T. Nishikawa, H. Shinokubo and K. Oshima, Tetrahedron, 2003, 59, 9661-9668.
-
(2003)
Tetrahedron
, vol.59
, pp. 9661-9668
-
-
Nishikawa, T.1
Shinokubo, H.2
Oshima, K.3
-
6
-
-
0344873803
-
-
2 with the Lindlar catalyst: W. M. Kwok, C. Ma, D. Phillips, A. Beeby, T. B. Marder, R. LI. Thomas, C. Tschuschke, G. Baranović, P. Matousek, M. Towrie and A. W. Parker, J. Raman Spectrosc., 2003, 34, 886-891.
-
(2003)
J. Raman Spectrosc.
, vol.34
, pp. 886-891
-
-
Kwok, W.M.1
Ma, C.2
Phillips, D.3
Beeby, A.4
Marder, T.B.5
Thomas, R.L.I.6
Tschuschke, C.7
Baranović, G.8
Matousek, P.9
Towrie, M.10
Parker, A.W.11
-
7
-
-
36549092073
-
-
3 in the Birch reduction: S. H. Courtney, M. W. Balk, L. A. Philips, S. P. Webb, D. Yang, D. H. Levy and G. R. Fleming, J. Chem. Phys., 1988, 89, 6697-6707.
-
(1988)
J. Chem. Phys.
, vol.89
, pp. 6697-6707
-
-
Courtney, S.H.1
Balk, M.W.2
Philips, L.A.3
Webb, S.P.4
Yang, D.5
Levy, D.H.6
Fleming, G.R.7
-
9
-
-
0010896917
-
-
(b) H. Sakurai, J. Abe and K. Sakamoto, Main Group Met. Chem., 1990, 13, 203-209;
-
(1990)
Main Group Met. Chem.
, vol.13
, pp. 203-209
-
-
Sakurai, H.1
Abe, J.2
Sakamoto, K.3
-
10
-
-
29644447217
-
-
ed. E. Negishi, Wiley, New York
-
(c) For a review, see: F. Sato, in Handbook of Organopalladium Chemistry for Organic Synthesis, ed. E. Negishi, Wiley, New York, 2002, pp. 2759-2765.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 2759-2765
-
-
Sato, F.1
-
11
-
-
29644436283
-
-
note
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2 in 89% deuterium ratio. See reference 3b.
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-
-
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12
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29644436470
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-
note
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1H NMR and GC/GC-MS, respectively.
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-
-
-
13
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0000596435
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2O. For the reaction of π-allylpalladium complexes with disilanes, see: Y. Tsuji, M. Funato, M. Ozawa, H. Ogiyama, S. Kajita and T. Kawamura, J. Org. Chem., 1996, 61, 5779-5787.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 5779-5787
-
-
Tsuji, Y.1
Funato, M.2
Ozawa, M.3
Ogiyama, H.4
Kajita, S.5
Kawamura, T.6
-
14
-
-
29644436378
-
-
ed. E. Negishi, Wiley, New York
-
For a review, see: Y. Tsuji, in Handbook of Organopalladium Chemistry for Organic Synthesis, ed. E. Negishi, Wiley, New York, 2002, pp. 1913-1916.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 1913-1916
-
-
Tsuji, Y.1
-
15
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29644436893
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-
2 to give ethoxysilanes with evolution of molecular hydrogen. Disilanes lacking a π-substituent are inert there. K. Yamamoto, M. Kumada, I. Nakajima, K. Maeda and N. Imaki, J. Organomet. Chem., 1968, 13, 329-341;
-
(1968)
J. Organomet. Chem.
, vol.13
, pp. 329-341
-
-
Yamamoto, K.1
Kumada, M.2
Nakajima, I.3
Maeda, K.4
Imaki, N.5
-
17
-
-
0142048736
-
-
For the palladium-catalyzed dehydrogenative coupling of hydrosilanes with alcohols to give alkoxysilanes, see: L. H. Sommer and J. E. Lyons, J. Am. Chem. Soc., 1967, 89, 1521-1522.
-
(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 1521-1522
-
-
Sommer, L.H.1
Lyons, J.E.2
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